Methanesulfonyl chloride → HCID 59655853, compound
Reaction equation
[NH2:1][CH2:2][CH2:3][C:4]1[CH:5]=[C:6]([Sn:10]([CH3:13])([CH3:12])[CH3:11])[CH:7]=[CH:8][CH:9]=1.[CH3:14][S:15](Cl)(=[O:17])=[O:16]>>[CH3:14][S:15]([NH:1][CH2:2][CH2:3][C:4]1[CH:5]=[C:6]([Sn:10]([CH3:12])([CH3:11])[CH3:13])[CH:7]=[CH:8][CH:9]=1)(=[O:17])=[O:16]Participants
3
Procedure
The title compound was prepared by the method of example 17, part A, from 3(2′-aminoethyl)phenyl trimethylstannane and methanesulfonyl chloride.
Sources & evidence
- ORD record
- ord-7602e58df786457392d6e798009fdd6d
- Source dataset
- uspto-grants-2008_02
- Patent number
- US07329668B2
Reaction notes
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